3-IODOBENZYL ALCOHOL

Names

[ CAS No. ]:
57455-06-8

[ Name ]:
3-IODOBENZYL ALCOHOL

[Synonym ]:
EINECS 260-744-9
MFCD00004635
(3-iodophenyl)methanol

Chemical & Physical Properties

[ Density]:
1.842 g/mL at 25 °C(lit.)

[ Boiling Point ]:
252 °C711 mm Hg(lit.)

[ Molecular Formula ]:
C₇H₇IO

[ Molecular Weight ]:
234.03400

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
233.95400

[ PSA ]:
20.23000

[ LogP ]:
1.78350

[ Index of Refraction ]:
n20/D 1.636(lit.)

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :: DO8318000

CHEMICAL NAME :: Benzyl alcohol, m-iodo-

CAS REGISTRY NUMBER :: 57455-06-8

BEILSTEIN REFERENCE NO. :: 3234821

LAST UPDATED :: 199612

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C7-H7-I-O

MOLECULAR WEIGHT :: 234.04

WISWESSER LINE NOTATION :: Q1R CI

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LDLo - Lowest published lethal dose

ROUTE OF EXPOSURE :: Intraperitoneal

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 750 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: JPMSAE Journal of Pharmaceutical Sciences. (American Pharmaceutical Assoc., 2215 Constitution Ave., NW, Washington, DC 20037) V.50- 1961- Volume(issue)/page/year: 67,1154,1978

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
DO8318000

[ HS Code ]:
2906299090

Precursor & DownStream

Precursor

DownStream

(3-(1H-PYRAZOL-3-YL)PHENYL)METHANOL
[3-(1H-PYRAZOL-1-YL)PHENYL]METHANOL
3-Iodobenzaldehyde
Methyl 3-iodobenzoate
1-(Chloromethyl)-3-iodobenzene
3-(3-Iodophenyl)propanoic acid
(3S,7AR)-3-T-BUTYL-7A-METHYLBICYCLICLACTAM
3-(3-methoxyphenyl)benzaldehyde
3-Hydroxybenzyl alcohol
(4-METHOXYBENZYL)HYDRAZINEDIHYDROCHLORIDE

Customs

[ HS Code ]: 2906299090

[ Summary ]:
2906299090 other aromatic alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

Dendritic metalloporphyrins with a distal H-bond donor as mimics of haemoglobin.

Org. Biomol. Chem. 1(7) , 1090-93, (2003)

We report the synthesis of iron(II) porphyrins functionalised with first- and second-generation dendrons as mimics of haemoglobin. The porphyrin core bears an ethynyl linker pointing towards the centr...

Radiolabeled guanine derivatives for the in vivo mapping of O(6)-alkylguanine-DNA alkyltransferase: 6-(4-[(18)F]Fluoro-benzyloxy)-9H-purin-2-ylamine and 6-(3-[(131)I]Iodo-benzyloxy)-9H-purin-2-ylamine.

Bioconjug. Chem. 11(6) , 868-75, (2000)

Two radiolabeled analogues of 6-benzyloxy-9H-purin-2-ylamine (O(6)-benzylguanine; BG) potentially useful in the in vivo mapping of O(6)-alkylguanine-DNA alkyltransferase (AGT) were synthesized. Fluori...

Direct synthesis of unprotected phenols using palladium-catalysed cross coupling reactions of functionalised organozinc reagents.

Org. Biomol. Chem. 2(1) , 110-13, (2004)

Palladium-catalysed reaction of unprotected 2-, 3-, and 4-iodophenols with a range of amino acid derived organozinc reagents (not used in excess) gives the expected products in good to excellent yield...

2-bromo-3-iodobenzyl alcohol
4-Bromo-3-iodobenzyl alcohol
5-bromo-3-iodobenzyl alcohol
4-amino-3-iodobenzyl alcohol
4-chloro-3-iodobenzyl alcohol
4-HYDROXY-3-IODOBENZYL ALCOHOL
3-(3-tert-butyl-1-methyl-1H-pyrazol-4-yl)-1-methyl-1H-pyrazol-5-amine
2-(2-Hydroxyphenyl)-4-(3-fluorophenyl)-6-(3-hydroxyphenyl)pyridine
4-methyl-4-{3H-[1,2,3]triazolo[4,5-b]pyridin-6-yloxy}piperidine
N-tert-butylmorpholine-4-carbohydrazide
(2R)-1-amino-4-fluorobutan-2-ol
2-[3-(Propan-2-yl)phenyl]cyclohexan-1-one
4-(2-Chloro-5-methoxyphenyl)morpholin-3-one
tert-butyl N-[5-(but-3-yn-1-yl)pyrimidin-2-yl]carbamate
2-(2-Nitroethyl)pyrazolo[1,5-a]pyrimidine
(2S)-1-[(2S)-3-cyclopropyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]piperidine-2-carboxylic acid

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.