167216-17-3

• 

• Basic information

  1. Product Name: Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)
  2. Synonyms: Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI);Boc-(R)-3-aminobutan-1-ol;N-Boc-(R)-3-aminobutan-1-ol;(R)-tert-Butyl (4-hydroxybutan-2-yl)carbamate;(R)-N-BOC-3-AMINOBUTAN-1-OL
  3. CAS NO:167216-17-3
  4. Molecular Formula: C₉H₁₉NO₃
  5. Molecular Weight: 189.25206
  6. EINECS: N/A
  7. Product Categories: N-BOC
  8. Mol File: 167216-17-3.mol
  9. Article Data: 12

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 301.4±25.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.010±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: 2-8°C
  8. Solubility: N/A
  9. PKA: 12.32±0.46(Predicted)
  10. CAS DataBase Reference: Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
  11. NIST Chemistry Reference: Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)(167216-17-3)
  12. EPA Substance Registry System: Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)(167216-17-3)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 167216-17-3(Hazardous Substances Data)

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• SDS
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• Downstream Products
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167216-17-3 Suppliers

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• Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)CAS NO.: 167216-17-3

  Cas No: 167216-17-3

• USD $ 5.0-5.0 / Kilogram

• 1 Kilogram

• 10000 Kilogram/Day

• Henan Wentao Chemical Product Co., Ltd.
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• (R)-N-BOC-3-AMINOBUTAN-1-OL

  Cas No: 167216-17-3

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• No Data

• No Data

• Suzhou Health Chemicals Co., Ltd.
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• N-β-t-Butoxycarbonyl-L-β-homoalaniol;(S)-3-[(t-Butoxycarbonyl)amino]-1-butanol

  Cas No: 167216-17-3

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• BOC Sciences
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• Carbamic acid,[(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)

  Cas No: 167216-17-3

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• Henan Tianfu Chemical Co., Ltd.
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• N-BOC-(R)-3-AMINOBUTAN-1-OL

  Cas No: 167216-17-3

• No Data

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• No Data

• Afine Chemicals Limited
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• Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)

  Cas No: 167216-17-3

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• ZHEJIANG JIUZHOU CHEM CO.,LTD
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• (R)-tert-Butyl (4-hydroxybutan-2-yl)carbamate

  Cas No: 167216-17-3

• No Data

• 10 Milligram

• Amadis Chemical Co., Ltd.
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• Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI)

  Cas No: 167216-17-3

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• ShenZhen InnoSyn Biotech Co.,Ltd
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167216-17-3 Usage

General Description

Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI) is a chemical compound with the molecular formula C9H19NO3. It is an ester of carbamic acid and is commonly known as (R)-tert-butyl 3-hydroxyisobutylcarbamate. Carbamic acid, [(1R)-3-hydroxy-1-methylpropyl]-, 1,1-dimethylethyl ester (9CI) is used in the pharmaceutical industry as an intermediate in the synthesis of various medications. It is also used in research and development for the production of new drugs. Additionally, this chemical may have potential applications in organic synthesis and as a reagent in various laboratory processes. It is important to handle this compound with care and in accordance with proper safety protocols due to its potential reactivity and toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 167216-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,2,1 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 167216-17:
(8*1)+(7*6)+(6*7)+(5*2)+(4*1)+(3*6)+(2*1)+(1*7)=133
133 % 10 = 3
So 167216-17-3 is a valid CAS Registry Number.

167216-17-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	(-)-tert-butyl [(R)-3-hydroxy-1-methylpropyl]carbamate

1.2 Other means of identification

Product number	-
Other names	(R)-tert-butyl (4-hydroxybutan-2-yl)carbamate

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:167216-17-3 SDS

167216-17-3Upstream product

• 161529-22-2 benzyl (S)-2-(N-t-butoxycarbonylamino)-4-iodobutanoate 
• 1047665-48-4 (+)-tert-butyl [(R)-1-methylprop-2-en-1-yl]carbamate 
• 159877-47-1 methyl 3-(R)-[N-(tert-butoxycarbonyl)amino]-propanoate 
• 159991-23-8 (R)-3-((tert-butoxycarbonyl)amino)butanoic acid 
• 24424-99-5 di-tert-butyl dicarbonate 
• 61477-40-5 (R)-3-amino-1-butanol 

167216-17-3Downstream Products

• 497861-77-5 (+)-tert-butyl [(R)-1-methyl-3-oxopropyl]carbamate 
• 61477-40-5 (R)-3-amino-1-butanol 

167216-17-3Relevant articles and documents

BICYCLIC COMPOUNDS

-

Paragraph 00505, (2020/10/28)

Provided herein are compounds and pharmaceutical compositions comprising said compounds that are useful for treating cancers. Specific cancers include those that are mediated by YAP/TAZ or those that are modulated by the interaction between YAP/TAZ and TEAD.

MACROCYCLIC COMPOUNDS AS TRK KINASE INHIBITORS AND USES THEREOF

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Paragraph 258, (2019/05/30)

The present disclosure describes novel TRK kinase inhibitors and methods for preparing them. The pharmaceutical compositions comprising such TRK kinase inhibitors and methods of using them for treating cancer, infectious diseases, and other disorders are also described.

Preparation method of (R)-3-aminobutanol

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Paragraph 0022; 0023; 0024, (2017/08/29)

The invention relates to the technical field of synthesis of drug intermediates and particularly relates to a preparation method of dolutegravir intermediate (R)-3-aminobutanol, comprising: using 3-(Boc-amino)butyric acid as a starting material, chirally splitting to obtain a compound of formula I; reducing with sodium borohydride and Lewis acid to obtain a compound of formula II; performing amino deprotection to obtain (R)-3-aminobutanol. The materials used herein are low in price and easy to obtain, the reaction conditions are mild, the safety is reliable, process stability is high, the yield is high, optical purity is high, and the preparation method is green and suitable for industrial production.

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